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Womens Laxative

Dosage form: tablet, coated
Ingredients: BISACODYL 5mg
Labeler: Kroger Company
NDC code: 30142-067

Medically reviewed by Drugs.com. Last updated on Nov 1, 2024.

Kroger 44-607

Active ingredient (in each tablet)

Bisacodyl USP, 5 mg

Purpose

Stimulant laxative

Uses
  • for temporary relief of occasional constipation and irregularity
  • this product generally produces bowel movement in 6 to 12 hours

Warnings

Do not use

if you cannot swallow without chewing.

Ask a doctor before use if you have
  • stomach pain, nausea or vomiting
  • a sudden change in bowel habits that lasts more than 2 weeks

When using this product
  • do not chew or crush tablet(s)
  • do not use within 1 hour after taking an antacid or milk
  • you may have stomach discomfort, faintness and cramps

Stop use and ask a doctor if
  • you have rectal bleeding or fail to have a bowel movement after use of a laxative. These could be signs of a serious condition.
  • you need to use a laxative for more than 1 week

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions
  • take with a glass of water
adults and children 12 years and overtake 1 to 3 tablets in a single daily dose 
children 6 to under 12 years take 1 tablet in a single daily dose
children under 6 years ask a doctor

Other information
  • TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
  • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
  • avoid excessive humidity
  • see end flap for expiration date and lot number

Inactive ingredients

acacia, ammonium hydroxide, calcium carbonate, carnauba wax, colloidal anhydrous silica, corn starch, D&C red #27 aluminum lake, FD&C blue #2 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, iron oxide black, lactose anhydrous, magnesium stearate, methylparaben, polydextrose, polyethylene glycol, polyvinyl acetate phthalate, povidone, propylene glycol, propylparaben, shellac glaze, simethicone, sodium alginate, sodium benzoate, sodium bicarbonate, stearic acid, sucrose, talc, titanium dioxide, triacetin, triethyl citrate

Questions or comments?

1-800-632-6900

Principal display panel

COMPARE TO the active ingredient in DULCOLAX® PINK®
*See bottom panel

NDC 30142-067-56

Kroger®

Women's
Laxative

Bisacodyl USP, 5 mg
Stimulant Laxative

Gentle, predictable
overnight relief

25
COMFORT COATED TABLETS

Actual Size

Our Pharmacists Recommend

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING

*Dulcolax® Pink® is a registered trademark of Boehringer Ingelheim Corporation. Plainsboro, NJ, 08536, Boehringer Ingelheim Corporation is not affiliated with The Kroger Co. or this product.

50844   REV0217A60756

DISTRIBUTED BY THE KROGER CO.
CINCINNATI, OHIO 45202

QUALITY GUARANTEE
www.kroger.com

Kroger 44-607

WOMENS LAXATIVE 
bisacodyl tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-067
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISACODYL (DEACETYLBISACODYL) BISACODYL5 mg
Inactive Ingredients
Ingredient NameStrength
ACACIA 
CALCIUM CARBONATE 
CARNAUBA WAX 
STARCH, CORN 
D&C RED NO. 27 
FD&C YELLOW NO. 6 
HYPROMELLOSE, UNSPECIFIED 
FERROSOFERRIC OXIDE 
MAGNESIUM STEARATE 
METHYLPARABEN 
POLYDEXTROSE 
POLYETHYLENE GLYCOL, UNSPECIFIED 
Polyvinyl Acetate Phthalate 
POVIDONE 
PROPYLENE GLYCOL 
PROPYLPARABEN 
SHELLAC 
SODIUM ALGINATE 
SODIUM BENZOATE 
SODIUM BICARBONATE 
STEARIC ACID 
SUCROSE 
TALC 
TITANIUM DIOXIDE 
TRIACETIN 
TRIETHYL CITRATE 
ANHYDROUS LACTOSE 
FD&C BLUE NO. 2 
SILICON DIOXIDE 
DIMETHICONE 
WATER 
AMMONIA 
Product Characteristics
ColorPINKScoreno score
ShapeROUNDSize6mm
FlavorImprint Code5
Contains    
Packaging
#Item CodePackage Description
1NDC:30142-067-561 BLISTER PACK in 1 CARTON
125 TABLET, COATED in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart33404/01/2013
Labeler - Kroger Company (006999528)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(30142-067)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867894MANUFACTURE(30142-067)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867837PACK(30142-067)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.967626305PACK(30142-067)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.868734088PACK(30142-067)

Revised: 11/2019
 
Kroger Company

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.